← Back to catalogue

Konar-Mf

EUDAMED

Class III (EU MDR)

Ref LT-MFO-6-4

by Lifetech Scientific (Shenzhen) Co., Ltd.

Identity

Trade Name
KONAR-MF EUDAMED
Device Name
KONAR-MF™ VSD Occluder EUDAMED
Model / Reference
LT-MFO-6-4 EUDAMED

Identifiers

Primary DI / UDI-DI
06938370104216 EUDAMED
Basic UDI-DI
B-06938370104216 EUDAMED
EMDN Code
P07040301 CARDIAC OCCLUDERS, VENTRICULAR SEPTAL DEFECTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Konar-Mf by Lifetech Scientific (Shenzhen) Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000001561
Authorised Representative
LifeTech Scientific (Europe) B.V. NL-AR-000000804

Sources (1)

  • EUDAMED 8ea6cbaa-cf16-4a7d-8616-4949686f4525 61 fields · synced Jun 18, 2026